|
HS Code |
938734 |
| Chemical Name | 2-Nitrophenol |
| Cas Number | 88-75-5 |
| Molecular Formula | C6H5NO3 |
| Molecular Weight | 139.11 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 44-46 °C |
| Boiling Point | 218 °C |
| Density | 1.481 g/cm3 |
| Solubility In Water | Moderate |
| Pka | 7.23 |
| Flash Point | 108 °C |
| Synonyms | o-Nitrophenol |
| Odor | Phenolic |
As an accredited 2-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Nitrophenol, 100g, supplied in an amber glass bottle with a tightly sealed cap and prominent hazard and safety labels. |
| Shipping | 2-Nitrophenol is shipped as a hazardous chemical due to its toxic and potentially combustible nature. It must be securely packed in airtight containers, clearly labeled, and comply with local and international transport regulations. Handle with care, avoiding heat, ignition sources, or mechanical shock during transit. Suitable protective measures must be observed. |
| Storage | 2-Nitrophenol should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizers and reducing agents. It should be kept in tightly closed, chemically compatible containers, labeled clearly, and protected from light. Always ensure proper containment to prevent leaks or spills and comply with relevant safety regulations. |
Applications of 2-Nitrophenol in Industrial ManufacturingAs a direct manufacturer of 2-Nitrophenol, we supply this intermediate to several critical industries where its reactivity and purity are fundamental to large-scale chemical synthesis. Below are key application tracks with specific integration details, compliance references, technical ratios, and downstream production endpoints. 1. Dye Intermediate Production (Azo and Sulfur Dyes Synthesis)Dye manufacturers use our 2-Nitrophenol primarily in the production of azo and sulfur dyes for textiles and paper. Its unique nitro group reactivity is crucial for forming azo linkages in chromophore structures. In batch processes, operators introduce 2-Nitrophenol in a controlled alkaline environment, ensuring selective coupling with diazonium salts. The purity specification supports consistent dye shade and solubility, directly affecting downstream quality control. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Pharmaceutical Synthesis (Paracetamol Precursors)Major API manufacturers incorporate 2-Nitrophenol during multi-step synthesis of paracetamol and related acetaminophen derivatives. Reduction yields 2-aminophenol, an essential building block in paracetamol route. Process engineers control stoichiometry tightly to remove excess nitro compound, supporting final pharmacopoeia validation. Direct integration into hydrogenation reactors allows monitored conversion under GMP environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Intermediate Manufacturing (Herbicide Syntheses)Agrochemical companies employ 2-Nitrophenol in the manufacture of specific phenolic herbicide actives. The nitro group supports effective ring substitution when forming precursor molecules such as 2-aminophenol derivatives, which later become core actives for broadleaf weed control agents. Process units require consistent supply and controlled addition to reaction vessels, followed by purification prior to formulation blending. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Chemical Analytical Reagent FormulationsAnalytical laboratories apply 2-Nitrophenol in colorimetric detection kits and chemical indicator preparations for trace metal analysis. The compound’s distinct absorbance profile allows precise calibration in spectrophotometric assays. Analysts prepare dilution standards for heavy metal determinations, benefiting from predictable optical performance and solubility characteristics in buffered solutions. Industry compliance standards
Typical usage ratio
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5. Rubber Chemical Additives (Antioxidant Synthesis)Producers of rubber processing chemicals utilize 2-Nitrophenol as a building block in the synthesis of select antioxidants employed during compounding of tires and industrial rubber parts. Its role, following reduction and further alkylation, is to provide phenolic segments that reduce oxidative degradation under high mechanical and thermal loads. Batch manufacturing processes require strict monitoring to prevent leftover nitro residues in the antioxidant agents. Industry compliance standards
Typical usage ratio
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With each batch leaving our reactors, 2-nitrophenol isn’t simply another inventory line but a product shaped by decades of hands-on processing, feedback from industrial partners, and the strictest batch-to-batch controls. Experience with 2-nitrophenol shows it serves as more than a chemical intermediate. Its consistent properties help specialty chemical companies avoid costly disruptions and hold tight specifications as they work towards demanding end products.
2-Nitrophenol, often identified by the molecular formula C6H5NO3, appears as a pale-yellow crystalline solid under standard conditions. Precision matters—over the years, we’ve received strict requests for minimum assay and maximum impurity content. Reliable performance hinges on purity, and the average industry standard lands above 99% content for 2-nitrophenol. Even a small shift in impurity profile brings major swings in reaction yield or color characteristics in downstream synthesis, especially in dyestuff applications and pharmaceutical intermediates.
Color holds special importance for many users. Trace amounts of related isomers or dinitro compounds can darken the product, shifting its purity by visual as well as analytical means. It takes experienced handling during nitration and purification steps to repeatedly achieve a bright-yellow powder, free from unwanted color-forming byproducts.
We’ve seen firsthand the product’s importance to the manufacture of azo dyes and couplers, particularly where robust nitroaromatic intermediates are needed. From fine-tuning color palettes to boosting performance in specialty coatings, 2-nitrophenol gives formulation chemists predictable results every time. In pharmaceutical synthesis, its controlled reactivity supports the production of antipyretic and analgesic agents. Most of our customers push for traceable quality control documentation because even marginally impure nitrophenol risks final product stability or safety.
Over the years, many laboratories and pilot plants have reported how substituting 2-nitrophenol for similar compounds like 4-nitrophenol or 3-nitrophenol yields stark differences in reaction rates and end properties. The ortho-nitro configuration brings unique reactivity—it is more acidic than its para- or meta-isomers, and this influences coupling and reduction steps in multi-stage synthesis. For chemists pursuing specific byproducts or derivatives, this positional effect enables them to steer processes with greater confidence.
We prepare 2-nitrophenol in granular and fine powder forms, tested and adapted over years to match dosing and feeding equipment in both batch and continuous reactors. Consistency in melting point (typically recorded in the 113–115°C range) and moisture content play as much of a role as analytical purity. Our QA team runs every lot against calibrated reference materials, reporting not only purity but also trace metal content, ash, and residual solvents. This vigilance cuts down on contamination risks, which commonly arise in large-scale production, not bench-scale trials.
Some facilities have requested higher packing density or dust-minimized granules to match sophisticated material handling systems. Pilot feedback showed where fluidity and dust suppression could improve the operator experience. Listening closely, we've tailored granulation size—without relying on binders that could introduce unwanted leachables or slow dissolution. For end-users exposed to 2-nitrophenol hour by hour, we ensure minimal dusting and easy dispersibility by direct granulation and air-jet milling, choices based on plant safety and housekeeping needs, as well as process performance.
Much confusion exists between 2-nitrophenol and its isomers. The position of the nitro group relative to the hydroxyl group truly controls its chemical character. Isomers such as 4-nitrophenol serve different purpose. Ortho nitrophenol, with the nitro group adjacent to the hydroxyl group, offers greater acidity and distinct UV-visible absorption. These subtle differences stand out in catalytic hydrogenation or when acting as a coupling agent for dyes and pigments. Missing the right isomer means risking entire batches or scrambling for revalidation in regulatory filings—a frustration many manufacturers have relayed to us.
We’ve observed customers turn away from mixed isomer products after encountering variable color development in dyes or unexpected impurity signals in pharmaceutical APIs. With 2-nitrophenol, there’s a sharper pH profile, especially useful for titration-based colorimetric analyses or applications demanding rapid, predictable benzene-ring substitution. In the case of environmental assay kits, only the ortho-isomer delivers the target absorbance spectrum at 438 nm, distinguishing itself from both meta and para alternatives. From a supply viewpoint, mistakenly sourcing a blend impacts the whole downstream process, often detected too late—after large-scale synthesis is under way. Our separation technology focuses on keeping isomer purity above 99%, supporting manufacturers who want less troubleshooting and fewer rejected lots.
Years ago, we learned that direct users care about more than just chemical specs—they count on consistency across shipments. One year, a small uptick in metal impurity from a raw material vendor cascaded down to cause slow catalyst poisoning in a Japanese customer’s dye plant. That incident drove a sharper focus on vendor auditing, in-process sampling, and real-time impurity mapping. Electrochemical and spectroscopic scans now flag deviations before they turn into returns or lost time for customers.
Handling safety arises in every batch. 2-nitrophenol, like many nitroaromatics, requires careful handling protocols. Our plant operators don full PPE, and our safety manuals include tried-and-true incident prevention measures based on both regulatory best practices and lessons from near misses. Regular training and maintenance of gas scrubbing systems and dust collectors ensure safety for both staff and downstream users who transfer, weigh, and react our 2-nitrophenol daily.
We see tumult in the global supply chain—rising input costs, energy volatility, stricter transportation rules—but predictability in 2-nitrophenol shipping remains critical to partners. We keep extra inventory to buffer volatility, storing drums in climate-stabilized warehouses and shipping with full batch traceability. By partnering closely with approved transporters familiar with hazardous materials, we’ve kept late deliveries and weather-based spoilage near zero. For critical supply projects, backup sourcing arrangements keep contract manufacturers and research plants running.
Feedback from the field reshapes our practices. Once, feedback from a dye user in Brazil noted mild, unexpected yellow-brown specks in formulated inks. Our technical group backtracked to a trace oxidative byproduct, tuning the final filtration process to reduce that impurity below visible limits. Another customer flagged slow dissolution in continuous reactors; our response was to invest in air-jet milling and adjust moisture tolerances to make the product not only more soluble, but also less likely to cake in automated feeders. These measures, adapted directly in our production lines, derived not from abstract guidelines but hands-on learning at scale.
Every step in making 2-nitrophenol intersects with customer process safety. We standardized on non-phthalate packaging, responding to regulatory shifts and customer audits, even though it forced changes in supplier base and internal handling. Surface treatments on drums and liners reduce static charge risks, informed by QRA studies and real-world transfer incidents in high-dust environments.
Our technical exchange does not end at the plant gate. Customers regularly consult our chemists about compatibility in mixed aromatic reactions, regulatory updates, or process optimization. Many partners turn to us for tailored guidance on storage and drum handling, or to troubleshoot unanticipated trace impurity breakthroughs affecting color precision. From time to time, we organize on-site visits and workshops to help industrial users get the most from our experience with 2-nitrophenol in diverse international settings.
We recognize the increasing demand for substance traceability and environmental responsibility. Our traceability system tracks every drum back to source lots, with digital batch reports accessible by customers. A routine example—switching a raw material grade can shift impurity spectra; by capturing real-time data and results, we give users the transparency needed for compliance documentation or troubleshooting in regulated markets. Our team works with various environmental health and safety standards, reporting regularly to local and global agencies, enabling customers to anticipate compliance shifts and fulfill downstream requirements involving 2-nitrophenol as a starting material.
Sustainable manufacturing sits on every agenda. With 2-nitrophenol, waste management presents real challenges due to combined nitro, phenolic, and aromatic environmental loads. We operate closed-loop recovery systems on-site to reclaim spent reaction liquors and minimize discharge. Our wastewater neutralization systems use advanced oxidation and monitored neutral pH points to keep effluent within regulatory limits. Regular audits ensure compliance remains ahead of environmental rule changes.
From the regulatory front, compliance means more than sending certificates. Our QA group audits each lot for conformity to local and international hazard classifications before release, clearing not only on purity and physical form, but also on transport document requirements. Hazard communication with all shipping paperwork remains streamlined, drawing on our decades of experience with nitroaromatic substances.
Where can 2-nitrophenol go next? Application scientists visit our facility each month to review performance enhancements. The next wave involves custom derivatives—sulfonated, halogenated, or aminated—is where many customers want to build new dyes, active pharmaceutical ingredients, or specialty monomers. Our teams conduct pilot programs and co-development trials so that users can translate lab-scale innovations into production-scale runs with confidence in batch scale-up and impurity control.
Even with a compound as mature as 2-nitrophenol, innovation continues. Feedback from global users, adaptation to shifting regulations, and a relentless focus on finished product performance all drive our process improvements. Fine adjustments in granulation, impurity management, and logistics support help manufacturers avoid the costly mistakes encountered with unknown or blended sources. As supply lines become more connected and accountable, the bar for technical support, safety, and transparency climbs ever higher. We welcome those challenges—each new batch reinforces a legacy of experience, responsiveness, and reliability for every downstream user that depends on 2-nitrophenol as a foundation for innovation.